Molecular analysis of phenylketonuria (PKU) in newborns from Texas by Yang, Y., Drummond-Borg, M., Garcia-Heras, J.

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Molecular Patterns of X Chromosome-Linked Color Vision Genes among 134 Men of European Ancestry by Drummond-Borg, Margaret, Deeb, Samir S., Motulsky, Arno G.

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Maternal complex chromosome rearrangement ascertained through a del (13)(q12.1q14.1) detected in her mildly affected daughter by Drummond-Borg, M., Kulharya, A.S., Tonk, V., Garcia-Heras, J.

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Molecular basis of abnormal red-green color vision: a family with three types of color vision defects by DRUMMOND-BORG, M, DEEB, S, MOTULSKY, A. G

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Classification of isolated versus multiple birth defects: An automated process for population‐based registries by Benjamin, Renata H., Nguyen, Joanne M., Drummond‐Borg, Margaret, Scheuerle, Angela E., Langlois, Peter H., Canfield, Mark A., Shumate, Charles J., Mitchell, Laura E., Agopian, A. J.

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Identifying syndromes in studies of structural birth defects: Guidance on classification and evaluation of potential impact by Benjamin, Renata H., Mitchell, Laura E., Scheuerle, Angela E., Langlois, Peter H., Canfield, Mark A., Drummond‐Borg, Margaret, Nguyen, Joanne M., Agopian, A. J.

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Newborn screening analytes and structural birth defects among 27,000 newborns by Lupo, Philip J, Archer, Natalie P, Harris, Rachel D, Marengo, Lisa K, Schraw, Jeremy M, Hoyt, Adrienne T, Tanksley, Susan, Lee, Rachel, Drummond-Borg, Margaret, Freedenberg, Debra, Shetty, Priya B, Agopian, A J, Shumate, Charles, Rasmussen, Sonja A, Langlois, Peter H, Canfield, Mark A

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Molecular patterns of X chromosome-linked color vision genes among 134 menof European ancestry by Drummond-Borg, M., Deeb, S.S., Motulsky, A.G.

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Epidemiology of Macrocephaly in the Texas Birth Defects Registry, 1999–2019 by Allred, Rachel P., Aguilar‐Martinez, J., Howell, R., Betancourt, Dayana, Marengo, Lisa, Dixon, A., Jeon, H., Yantz, C., Kilburn, M., Drummond‐Borg, Margaret, Nguyen, Joanne, Arena, Fernando, Shumate, Charles

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The Impact of Transient Hypothyroidism on the Increasing Rate of Congenital Hypothyroidism in the United States by PARKS, John S, LIN, Michelle, GROSSE, Scott D, HINTON, Cynthia F, DRUMMOND-BORG, Margaret, BORGFELD, Lynette, SULLIVAN, Kevin M

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Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism by Harms, Frederike Leonie, Girisha, Katta M., Hardigan, Andrew A., Kortüm, Fanny, Shukla, Anju, Alawi, Malik, Dalal, Ashwin, Brady, Lauren, Tarnopolsky, Mark, Bird, Lynne M., Ceulemans, Sophia, Bebin, Martina, Bowling, Kevin M., Hiatt, Susan M., Lose, Edward J., Primiano, Michelle, Chung, Wendy K., Juusola, Jane, Akdemir, Zeynep C., Bainbridge, Matthew, Charng, Wu-Lin, Drummond-Borg, Margaret, Eldomery, Mohammad K., El-Hattab, Ayman W., Saleh, Mohammed A.M., Bézieau, Stéphane, Cogné, Benjamin, Isidor, Bertrand, Küry, Sébastien, Lupski, James R., Myers, Richard M., Cooper, Gregory M., Kutsche, Kerstin

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The impact of transient hypothyroidism on the increasing rate of congenital hypothyroidism in the United States.(The Increasing Incidence of Congenital Hypothyroidism in the United... by Parks, John S, Lin, Michelle, Grosse, Scott D, Hinton, Cynthia F, Drummond-Borg, Margaret, Borgfeld, Lynette, Sullivan, Kevin M

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